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微针联合树突状细胞靶向纳米疫苗递送系统在三阴性乳腺癌经皮免疫治疗中的应用

Application of microneedles combined with dendritic cell-targeted nanovaccine delivery system in percutaneous immunotherapy for triple-negative breast cancer.

作者信息

Weng Jiaqi, Yang Jing, Wang Weiwei, Wen Jiaoli, Fang Min, Zheng Gensuo, Xie Jing, Zheng Xi, Feng Lili, Yan Qinying

机构信息

College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou 310014, People's Republic of China.

Third Clinical College of Wenzhou Medical University, Wenzhou People's Hospital, Wenzhou 325000, People's Republic of China.

出版信息

Nanotechnology. 2023 Sep 5;34(47). doi: 10.1088/1361-6528/ace97b.


DOI:10.1088/1361-6528/ace97b
PMID:37478829
Abstract

This work aims at developing a strategy to activate the antigen-presenting cells to enhance the effect of immunotherapy in triple-negative breast cancer (TNBC) through the dissolving microneedle patch (DMNP). In present study, mannosylated chitosan (MCS) nanoparticles (NPs) were designed to target dendritic cells (DCs), and the immunotherapy effect was enhanced by the adjuvant Bacillus Calmette-Guerin polysaccharide (BCG-PSN), achieving the purpose of transdermal immunotherapy for TNBC. Vaccination studies with mice demonstrated that MCS NPs effectively induce DCs maturation in the tumor-draining lymph nodes to stimulate strong immune responses in TNBC. Overall, chitosan-based DMNPs with complex adjuvant constituted a new potent transdermal vaccine delivery platform capable of exploiting more DCs in the skin for effective immunization.

摘要

这项工作旨在开发一种策略,通过溶解微针贴片(DMNP)激活抗原呈递细胞,以增强三阴性乳腺癌(TNBC)免疫治疗的效果。在本研究中,设计了甘露糖基化壳聚糖(MCS)纳米颗粒(NPs)来靶向树突状细胞(DCs),并通过卡介苗多糖(BCG-PSN)佐剂增强免疫治疗效果,实现TNBC的经皮免疫治疗目的。对小鼠的疫苗接种研究表明,MCS NPs能有效诱导肿瘤引流淋巴结中的DCs成熟,从而在TNBC中激发强烈的免疫反应。总体而言,具有复合佐剂的基于壳聚糖的DMNPs构成了一个新的有效的经皮疫苗递送平台,能够利用皮肤中更多的DCs进行有效免疫。

相似文献

[1]
Application of microneedles combined with dendritic cell-targeted nanovaccine delivery system in percutaneous immunotherapy for triple-negative breast cancer.

Nanotechnology. 2023-9-5

[2]
Combination Immunotherapy of MUC1 mRNA Nano-vaccine and CTLA-4 Blockade Effectively Inhibits Growth of Triple Negative Breast Cancer.

Mol Ther. 2017-12-5

[3]
Nanoparticle-integrated dissolving microneedles for the co-delivery of R848/aPD-1 to synergistically reverse the immunosuppressive microenvironment of triple-negative breast cancer.

Acta Biomater. 2024-3-1

[4]
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Biomaterials. 2020-3

[5]
Enhanced antitumor immunity by targeting dendritic cells with tumor cell lysate-loaded chitosan nanoparticles vaccine.

Biomaterials. 2016-10-29

[6]
Targeted Codelivery of an Antigen and Dual Agonists by Hybrid Nanoparticles for Enhanced Cancer Immunotherapy.

Nano Lett. 2019-3-21

[7]
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Acta Biomater. 2023-3-1

[8]
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J Nanobiotechnology. 2023-9-26

[9]
Phenotypic profile of dendritic and T cells in the lymph node of Balb/C mice with breast cancer submitted to dendritic cells immunotherapy.

Immunol Lett. 2016-9

[10]
Self-assembly nanovaccine containing TLR7/8 agonist and STAT3 inhibitor enhances tumor immunotherapy by augmenting tumor-specific immune response.

J Immunother Cancer. 2021-8

引用本文的文献

[1]
Exosomal Mediates Immune Evasion in Triple-Negative Breast Cancer by Suppressing Dendritic Cell Activation via .

Iran J Public Health. 2025-6

[2]
Advances in clinical applications of microneedle.

Front Pharmacol. 2025-6-26

[3]
Sustained release microneedle patch for pronounced systemic delivery of doxazosin mesylate.

Bioimpacts. 2024-8-3

[4]
Chitosan non-particulate vaccine delivery systems.

J Pharm Pharm Sci. 2024-7-24

[5]
The quest for nanoparticle-powered vaccines in cancer immunotherapy.

J Nanobiotechnology. 2024-2-14

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